Canonical Allele Identifier: PA2825139946
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 866150
ClinVar Variation Id: 907108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000274.3:p.Thr604Ser
CA355917549
NM_000283.4:c.1810A>T
CA355917556
NM_000283.4:c.1811C>G